Park Hye-Rim, Min Soo Kee, Cho Hyun Deuk, Cho Sung Jin, Lee Jong Hyuk, Lee Yeol, Park Yong-Koo
Department of Pathology, College of Medicine, Hallym University, Anyang, Korea.
Skeletal Radiol. 2004 May;33(5):291-4. doi: 10.1007/s00256-003-0742-x. Epub 2004 Feb 18.
A rare case of chondroblastic osteosarcoma arising from the ethmoid sinus is reported. The patient, a 34-year-old woman, presented with diminished visual acuity of the left eye. CT and MR imaging showed a heterogeneous left-sided nasoethmoidal mass destroying the medial orbital wall. Biopsy revealed a chondroblastic osteosarcoma containing malignant chondroid elements and calcified malignant osteoid. Treatment consisted of craniofacial resection followed by radiotherapy and chemotherapy with symptomatic improvement. We briefly discuss ethmoidal osteosarcomas.
报告了一例罕见的起源于筛窦的软骨母细胞性骨肉瘤。患者为一名34岁女性,表现为左眼视力下降。CT和磁共振成像显示左侧鼻筛部有一不均匀肿块,破坏了眶内侧壁。活检显示为软骨母细胞性骨肉瘤,含有恶性软骨样成分和钙化的恶性骨样组织。治疗包括颅面切除术,随后进行放疗和化疗,症状有所改善。我们简要讨论筛窦骨肉瘤。